Arco C Siremobil

SP

Chequeo de imagen

SIREMOBIL Compact L © Siemens AG 1997

The reproduction, transmission or
SIREMOBIL Compact as of use of this document or its contents
is not permitted without express
written authority. Offenders will be

Serial Number 02001 liable for damages. All rights,

including rights created by patent
grant or registration of a utility
model _or_ design,_are_ reserved.

Register 5 English
Print No.: SPR2-11.3432.3543. Doc. Gen. Date: 01.0
Replaces: SPR2-130.037.01.03.02
0-2 Revision

Chapter Page Revision

0 - 12 all 04

SIREMOBIL Compact / L Register 5 SPR2-130.037.01 Page 2 of 4 Siemens AG

Log book Rev. 04 01.06 CS PS SP Medical Engineering
Contents 0-3

Page
1 _______System identification and Test requirements ________________________ 1 - 1

System identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-1

Required measuring instruments and devices . . . . . . . . . . . . . . . . . . . . .1-2
Test requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Parameters of the organ program for performing the IQ quick test . . . . . . . . .1-3

2 _______Checking the ADR curves________________________________________ 2 - 1

Checking the ADR curves . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-1

Prerequisites. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-1
Evaluation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2- 2
ADR curves for fluoroscopy operating mode . . . . . . . . . . . . . . . . . . . .2-2
ADR curves for pulsed fluoroscopy operating mode . . . . . . . . . . . . . . . .2-3
ADR curves for DR operating mode . . . . . . . . . . . . . . . . . . . . . . . .2-4

3 _______Capillary test __________________________________________________ 3 - 1

Capillary test for Memoskop C-SUB, Memoskop C-SUB & Mod or Memoskop CX200 with
option DSA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Subtraction mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Roadmap Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4

4 _______Memoskop functional checks ____________________________________ 4 - 1

Edge enhancement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Noise reduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Motion detector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

5 _______Resolution ____________________________________________________ 5 - 1

Checking the resolution and the minimum contrast . . . . . . . . . . . . . . . . . . . 5 - 1

6 _______Checking the control systems ____________________________________ 6 - 1

Programming the previous noted values of the organ programs . . . . . . . . . . . . 6 - 2

7 _______Image artifacts _________________________________________________ 7 - 1

Image artifacts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-1

Definition of the rating numbers . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-1
Description of the artifacts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-1
Image artifacts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-2
Other artifacts:. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-2

8 _______Customer specific organ programs________________________________ 8 - 1

Programming the organ programs. . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

SIREMOBIL Compact without keyboard. . . . . . . . . . . . . . . . . . . . . . . 8 - 1
SIREMOBIL Compact with keyboard . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

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0-4 Contents

Page
Checking the newly programmed ADR control curves . . . . . . . . . . . . . . . . . 8-1
Prerequisites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1
Procedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Evaluation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2

9 ______ Multispot 2000 _________________________________________________9 - 1

Functional check at the factory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-1

Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-1
Setting the multiformat camera at the customer's site . . . . . . . . . . . . . . . . . 9-3
Multispot 2000-2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
Multispot 2000 1/4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
Checking the Multispot resolution . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
Prerequisites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
Multispot 2000-2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
Multispot 2000-1/4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-7

10 _____ Final Steps ____________________________________________________1 - 1

11 _____ Appendix ____________________________________________________11 - 1

Calling up the Memoskop test patterns. . . . . . . . . . . . . . . . . . . . . . . . .11 - 1

Memoskop CE / CE100 / C / C-SUB / C-SUB & MOD with keyboard . . . . . . .11 - 1
Memoskop CE without keyboard . . . . . . . . . . . . . . . . . . . . . . . . . .11 - 1
Memoskop CX200 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11 - 1
Standard programming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11 - 2
MEMOSKOP CE / CE100 / C / C-SUB / C-SUB & MOD . . . . . . . . . . . . . .11 - 2
MEMOSKOP CX200 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11 - 4

12 _____ Changes to previous version ____________________________________12 - 1

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Log book Rev. 04 01.06 CS PS SP Medical Engineering
System identification and Test requirements 1 1-1

System identification 1

Part No.: ______________ Serial No.: _____________________

Cust./Clinic: ________________________________________________
Address: ______________ City: ________________________
Country: ______________ State: ________________________
Telephone No.: ______________ Cont. person: __________________
System No.: ______________ Branch: _______________________
Responsible system engineer: ______________________________

Image quality acceptance performed completely in the factory and documented by:
Name (block capitals): __________________ Department:__________________
Signature: __________________ Date: __________________

Date of installation of the system at the customer's site: _______________

Image quality quick test performed in connection with:

Turnover to customer:
Maintenance:

Adjustments deviating from standard due to:

Country-specific regulations Special customer request
Reason: __________________________________________________________
_________________________________________________________________

Name (block capitals): __________________ Regional office: ______________

Signature: __________________

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1-2 System identification and Test requirements

Required measuring instruments and devices 1

• Set of X-radiation filters 10 x 0.3 mm Cu e.g. 44 06 120 RV090

• 2.1 mm Cu precision X-radiation filter 99 00 598 XE999

• 25 mm Al spacer, Type 26765 acc. to DIN 6868 Part 50

or
1.2 mm Cu from the radiation filter set 97 98 596 G5321 and
17 µm Cu - strip 11 67 662 G5247

• Set of resolution test patterns 28 71 820 RE999

Factory: Resolution test Type 41a

• Densitometer e.g. X-Rite 331 97 02 416 Y1996

or PTW-BC21 including Black-Check
Type 5321 and Light box Type 53213

TV dynamic range test kit 37 90 156 X1963

or 97 50 001 X1963
contains: TV dynamic test 37 90 164 X1963
Heart contour diaphragm 37 90 172 X1963
Capillary test 37 90 180 X1963
Holder 87 13 901 X1963
Lead step test 87 09 743 X1963

• Protective conductor meter e.g. Safety Tester Unimet 1100 51 38 727 Y0766

• Service PC

• Service Software SIREMOBIL Compact

• Service PC-SIREMOBIL serial interface cable 99 00 440 RE999

or 96 60 978 RE999

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Log book Rev. 04 01.06 CS PS SP Medical Engineering
System identification and Test requirements 1-3

Test requirements 1

• The entire system must be functioning properly; in addition, make sure that the
- grid,
- X-ray I.I. cover, and
- Sirephos cover (without DHHS spacer) are installed.
• If the nominal values are not attained, the system must be adjusted or repaired according
to the service instructions.
• Mark the appropriate boxes y/n with "y" for yes or "n" for no.

Parameters of the organ program for performing the IQ quick test 1

• Corresponding to the following table, in each case one of the available organ programs
has to be programmed temporarily for the existing operating modes.
• Note the parameter values in the organ programs previously and reprogram them after
completion of the IQ quick test.
• Perform programming according to the operating instructions of the system.
• Perform the tests in chapters 2 to 6 with the programmed values stated in the table.

NOTICE All parameters in normal type correspond to the programming of

the factory setting (default programming).
As long as the organ program 1 in the corresponding operating
modes still corresponds to the factory setting, only the parame-
ters marked with
*1 (for Memoskop CE /CE100 /C /C-SUB /C-SUB & MOD)
or
*2 (for Memoskop CX200)
need to be temporarily reprogrammed.

Organ program for performing the IQ quick test

Operating mode DL IDL DR SUB Roadmap
Program name Standard Standard Standard Standard Standard
Doserate MID MID MID *1 HIGH HIGH

SIREMATIC normal HC1 *2 HC1 *2 n.a. n.a. n.a.

(Iodine) (Iodine)
SIREMATIC push HC2 HC2 n.a. n.a. n.a.
Noise red. Low MD1 *2 K = 4 K=8 n.a. n.a.
(K4:K1)
Noise red. High MD2 K=8 K = 16 n.a. n.a.
(K16:K2)
Dose reduction low n.a. high n.a. n.a. n.a.
Dose reduction high n.a. high *2 n.a. n.a. n.a.

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1-4 System identification and Test requirements

Auto LIH disk transfer NO NO n.a. n.a. n.a.

Auto transfer each image n.a. NO n.a. n.a. n.a.
Disk transfer rate 0 n.a. n.a. n.a. n.a.
Auto disk transfer n.a. NO YES n.a. n.a.
Subtraction n.a. n.a. n.a. MAX MAX
Landmark n.a. n.a. n.a. NO NO
Video signal at docum. n.a. n.a. n.a. POS POS
Image display n.a. n.a. n.a. POS POS
Duration of the phase B1 n.a. n.a. n.a. 0 sec n.a.
Disk transfer rate (Phase B1) n.a. n.a. n.a. 0 n.a.
Disk transfer rate (Phase B2) n.a. n.a. n.a. 3 n.a.

*1 MEMOSKOP CE / CE100 ( C ( C-SUB 7 C-SUB&MOD: Values of the parameters for

performing the IQ quick test deviate from the standard programming of the organ pro-
grams (factory setting).
*2 MEMOSKOP CX200: Values of the parameters for performing the IQ quick test deviate
from the standard programming of the organ programs (factory setting.
*3 Organ Program 1: Program name if Memoskop C-SUB / C-SUB&MOD is installed.
*4 Organ Program 1: Program name if Memoskop CX200 is installed.

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Log book Rev. 04 01.06 CS PS SP Medical Engineering
Checking the ADR curves 2 2-1

Checking the ADR curves 2

Prerequisites 2

• When performing the following tests for the operating modes fluoroscopy, pulsed
fluoroscopy and DR. program the parameters in accordance to the specification in
chapter 1 , paragraph Test requirements.
• Attach the 2.1mm Cu precision radiation filter for prefiltration at the X-ray port on the tube
assembly.
• Select "Mid" as the dose level; this corresponds to
0.220 µGy/s ±15% for a 17 cm I.I. with survey format or
0.185 µGy/s ±15% for a 23 cm I.I. with survey format.

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2-2 Checking the ADR curves
Evaluation 2

NOTICE Check the ADR curves corresponding to those stated in

chapter 1, Test requirements paragraph. If different ADR curves
should be programmed at the customer’s request, firstly program
and test the curves stated in chapter 1, Test requirements para-
graph, to make sure by comparison that nothing has changed in
the system after delivery from the factory.
The curves available in the operating mode selected in each case
can be selected with the mA button.

ADR curves for fluoroscopy operating mode 2

• Test requirements: See chapter 1.

• Select and image intensifier full image format.
• Select Sirematic HC 1 ADR curve; the LED of the mA button is off.
• Radiation on.
• Read the indicated kV and mA values on the control panel.
• Radiation off.
• Enter the values in Tab. 1.
• Select Sirematic HC 2 ADR curve; the LED of the mA button is on.
• Radiation on.
• Read the indicated kV and mA values on the control panel.
• Radiation off.
• Enter the values in Tab. 1.
• The actual values documented in the factory must be reproduced at the application site.
Permissible deviations: Tube voltage (kV) ± 1kV, tube current (mA) ± 10%.

ADR curves Nominal values Actual values

fluoroscopy (Factory) Factory Application site
KV mA KV mA KV mA
Sirematic HC 1 63 - 68 KV 1.9 - 3.8 mA
Sirematic HC 2 61 - 66 KV 2.1 - 4.7 mA
Tab. 1

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Log book Rev. 04 01.06 CS PS SP Medical Engineering
Checking the ADR curves 2-3
ADR curves for pulsed fluoroscopy operating mode 2

• Test requirements: See chapter 1.

• Select and image intensifier full image format.
• Select Sirematic HC 1 ADR curve; the LED of the mA button is off.
• Radiation on.
• Read the indicated kV and mA values on the control panel.
• Radiation off.
• Enter the values in Tab. 2.
• Select Sirematic HC 2 ADR curve; the LED of the mA button is on.
• Radiation on.
• Read the indicated kV and mA values on the control panel.
• Radiation off.
• Enter the values in Tab. 2.
• The actual values documented in the factory must be reproduced at the site.
Acceptable deviations: Tube voltage (kV) ± 1kV, tube current (mA) ± 10%.

ADR curves Nominal values Actual values

pulsed (Factory)
Factory Application site
fluoroscopy
KV mA KV mA KV mA
Sirematic HC 1 63 - 68 KV 1.9 - 3.8 mA
Sirematic HC 2 61 - 66 KV 2.1 - 4.7 mA
Tab. 2

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2-4 Checking the ADR curves
ADR curves for DR operating mode 2

• Test requirements: See chapter 1.

• Select DR and image intensifier full format.
• Radiation on.
• Read the indicated kV and mA values on the control panel.
• Radiation off.
• Enter the values in Tab. 3.
• The actual values documented in the factory must be reproduced at the application site.
Acceptable deviations: Tube voltage (kV) ± 1kV, tube current (mA) ± 10%.

ADR curves Nominal values Actual values

DR (Factory)
Factory Application site
KV mA KV mA KV mA
DR 850W 61 - 66 KV 2.7 - 6.5 mA
Tab. 3

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Log book Rev. 04 01.06 CS PS SP Medical Engineering
Capillary test 3 3-1

NOTICE The dynamic test in conjunction with the Plexi capillary test is
used to display small differences in contrast.

• Test arrangement
- Remove the 2.1 mm radiation filter from the beam path.
- Attach the dynamic test without the holder but with heart contour diaphragm and Plexi
capillary test directly in front of the image intensifier input (Plexi capillaries close to X-
ray image intensifier).
• Prerequisites:
- Test requirements: See chapter1.
- Select FLUORO ( button) standard settings (refer to Appendix)
- Select Sirematic HC1. (LED in the mA button is off.)
- Select full format.
- Select high noise reduction, the LED of the button is off.
- Edge enhancement ( button) off.
- Select LUT 1.
- Switch on radiation and evaluate the live image.
• Evaluation of the monitor image
- Nominal value
The unmarked Plexi capillaries in Fig. 1a must be visible.
- Cross off Plexi capillaries in Fig. 1b that are not visible.
.
Nominal value Factory Application site
Group
3 mm * * * * * *
wide

2 mm
wide

1 mm
wide

Fig.1a Fig.1b Fig.1c

* Cannot be evaluated/not applicable for 17HDR-C image intensifier

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3-2 Capillary test

Capillary test for Memoskop C-SUB, Memoskop C-SUB & Mod or

Memoskop CX200 with option DSA 3

Memoskop C-SUB oder Memoskop C-SUB &Mod y/n

or Memoskop CX200 is present:

If no, omit the capillary test for Memoskop C-SUB, Memoskop C-SUB & Mod or
MemoskopCX200.

Subtraction mode 3

Measurement setup
• Attach the dynamic test without the holder but with the heart contour diaphragm and
Plexi capillary test directly in front of the image intensifier input (Plexi capillaries close to
image intensifier).

NOTICE For 17 cm (7") image intensifiers, the upper line of the 3mm group
can only be evaluated if the test is shifted slightly downward.

Prerequisites
• Test requirements: See chapter1.
• Select SUB.
• Use the following settings:
- Dose rate level "High" = 0.44 µGy/s ±15% for 17cm (7") I.I. or
0.37µGy/s ±15% for 23cm (9") I.I..
- Noise reduction for mask k = 32.
- Noise reduction for fill k = 16.
- SUB Phase A time 3 seconds.
• Select full format.
• Edge enhancement off.

Procedure
• Release the scene (radiation on).
• After E3 seconds, the mask is automatically placed. The "Inject" message appears on
the monitor.
• Start the Plexi capillary test by pressing the rubber ball.
• Shut off radiation after 3 seconds.

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Log book Rev. 04 01.06 CS PS SP Medical Engineering
Capillary test 3-3
Evaluation 1
• Select LUT 4.
• Find the capillary lines to be evaluated on monitor B in the individual matrix fields. They
should be separated according to black and white.

NOTICE Do not evaluate the first white line. Start the evaluation with the
first black line.

• Enter the results in table 1 and table 2. If a line is not recognizable, identify it with x.

Nominal values Factory Site

2L 1 5R 2L 1 5R 2L 1 5R Group
Black upper
group
Black X
3 mm
Black X X X wide
Black middle
group
Black X X
2 mm
Black X X X wide
Black lower
group
Black X
1 mm
Black X X X wide
Tab. 1

Nominal values Factory Site

2L 1 5R 2L 1 5R 2L 1 5R Group
White upper
group
White X X
3 mm
White X X X wide
White middle
group
White X X
2 mm
White X X X wide
White lower
group
White X
1 mm
White X X X wide
Tab. 2

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3-4 Capillary test
Evaluation 2
• Evaluate the 3mm white capillary lines in the 2L, 1 and 5R fields on monitor B.
No obvious brightness differences should be visible between the fields.
No obvious brightness differences Factory Site
are visible in fields 2L, 1 and 5R: y/n y/n

• Evaluate the 3mm black capillary lines in fields 2L, 1 and 5R on monitor B.
No obvious brightness difference should be visible between the fields.
No obvious brightness differences Factory Site
are visible in fields 2L, 1 and 5R: y/n y/n

Roadmap Mode 3

Measurement setup
• Attach the dynamic test without the holder but with the heart contour diaphragm and
Plexi capillary test directly in front of the I.I. input (Plexi-capillaries close to image
intensifier).

NOTICE For 17 cm (7") image intensifiers, the upper line of the 3mm group
can only be evaluated if the test is shifted slightly downward.

Prerequisites
• Test requirements: See chapter 1.
• Select Roadmap.
• Use the following settings:
- Dose rate level "Mid" = 0.22µGy/s ±15% for 17cm (7") I.I. or
0.185µGy/s ±15% for 23cm (9") I.I..
- Noise reduction for phase 1(K1) k = 16.
- Noise reduction for phase 2 (K2) k = 8
- Noise reduction for phase 3 (K3) k = 4
- Roadmap Phase A time 3 seconds.
• Select full format.
• Edge enhancement off.

Procedure
• Release the scene (radiation on; Phase 1)
• After>= 3 seconds, the mask is automatically placed. The "Inject" message appears on
the monitor.
• Do not shift the Plexi-capillaries. (radiation remains on; Phase 2)
• Shut off radiation after 3 more seconds.
• Release radiation again. (Phase 3)
• Start the Plexi-capillary test by pressing the rubber ball.
• Shut radiation off after 3 more seconds.

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Log book Rev. 04 01.06 CS PS SP Medical Engineering
Capillary test 3-5
Evaluation
• Select LUT 4.
• Find the capillary lines to be evaluated on monitor B in the individual matrix fields. They
should be separated according to black and white.

NOTICE Do not evaluate the first white line. Start the evaluation with the
first black line.

• Enter the results into table 3 and table 4. If a line is not identifiable, mark it with x.

Nominal values Factory Site

2L 1 5R 2L 1 5R 2L 1 5R Group
Black upper
group
Black X X
3 mm
Black X X X wide
Black middle
group
Black X X X
2 mm
Black X X X wide
Black lower
group
Black X X
1 mm
Black X X X wide
Tab. 3

Nominal values Factory Site

2L 1 5R 2L 1 5R 2L 1 5R Group
White upper
group
White X X X
3 mm
White X X X wide
White middle
group
White X X X
2 mm
White X X X wide
White lower
group
White X X
1 mm
White X X X wide
Tab. 4

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3-6 Capillary test
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Memoskop functional checks 4 4-1
• Prerequisites:
- Test requirements: See chapter 1.
- Attach the dynamic test without the holder but with the heart contour diaphragm and
Plexi capillary test directly in front of the image intensifier input (Plexi capillaries close
to the X-ray image intensifier).
- Select FLUORO
- Contrast setting for monitors - step 1 (LUT = 1)
- Edge enhancement = 0

Edge enhancement 4

- Switch fluoroscopy on briefly. The LIH image is visible on the monitor.

- Press the button for edge enhancement several times.
The 2 levels of edge enhancement are selected consecutively. (Edge enhancement off
- Edge enhancement stage 1 - Edge enhancement stage 2...)
Factory Application
site
- Edge enhancement function test o.k.? y/n y/n
(The bright - dark transitions become clearly visible
when selecting level 1 or 2)

Noise reduction 4

- Press the button for selecting the noise reduction factor; ; the LED of the button
must light up (low noise reduction).
- Switch fluoroscopy on briefly and assess the noise impression of the image during
radiation.
- Press the button for selecting the noise reduction factor; ; the LED of the button is
off (high noise reduction).
- Switch fluoroscopy on briefly and assess the noise impression of the image with
radiation on.
Factory Application
site
- Noise reduction functioning o.k.? y/n y/n
Image noise is less with the LED of the
button off ).

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4-2 Memoskop functional checks

Motion detector 4

NOTICE Perform this test only in the factory.

• Prerequisites:
- Test requirements: See chapter 1.
- Select FLUORO
- Select low noise reduction (MD1) ; the LED in the button is on.
- In addition, place a screwdriver centrally on the dynamic test.
- Radiation "ON"
- When activating the key for image rotation, the live image shows only a slight trailing
effect.
The image noise is more clearly visible in the moving parts of the image.
- Radiation "OFF"
- Select high noise reduction (MD2); the LED in the button is out.
- Radiation "ON"
- When activating the key for image rotation, the live image shows a greater trailing
effect than for low noise reduction.
The image noise is more clearly visible in the moving parts of the image.
- Radiation "OFF"
- Remove the screwdriver from the image intensifier.

- Evaluation of the monitor image.

Factory

- Motion detection o.k.? y/n

Trial effect vs. image noise)

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Resolution 5 5-1

Checking the resolution and the minimum contrast 5

• Prerequisites:
- Test requirements: See chapter 1.
- Select FLUORO and the "Mid" dose rate level.
- Select Sirematic HC1 ADR curves; LED of the mA button is off.
- Set edge enhancement to optimum detection of resolution.
- Press the button for noise reduction ; the LED of the button must be off.
- Set the contrast (LUT) for the monitors to optimum recognition of resolution.
- Factory: Use resolution test Type 41 A.
- Application site: Use resolution text Type 41.
Attach the resolution test directly to the grid in the center of the image intensi-
fier. It should be located at an angle of approximately 45° to the grid lines.
- Factory:
Attach 25 mm AL measuring stand to the image intensifier.
- Application site:
If a 25 mm AL measuring stand is present (with 0.4 mm notch) attach this
close to the image intensifier.
Otherwise:
Attach the 17 µm Cu strip directly to the grid next to the resolution test and
place an additional 1.2 mm Cu filtration in the beam path, close to the tube.
- If overframing occurs at the edge of the image intensifier, eliminate this with
collimation.
- Switch radiation "ON". Determine the resolution of the LIH image and enter it in Tab 1.
- In each case, check that the minimum contrast is detectable. (Notch in 25 mm AL or 17
µm Cu strip.)
• Evaluation
- Determine the line pairs/mm and enter the value in table 1.

Nominal resolution Actual resolution values [Lp/mm]

Operating Image inten- values [Lp/mm]
Factory Application site
mode sifier format
7" (17cm) 9" (23cm) Monitor 1 Monitor 2 Monitor 1 Monitor 2

during Full format ≥ 1.4 ≥ 1.2 n.a. n.a.

radiation

during Zoom ≥ 2.2 ≥ 1.6 n.a. n.a.

radiation

Full format ≥ 1.4 ≥ 1.2

LIH

Zoom ≥ 2.2 ≥ 1.6

LIH

Tab. 1

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5-2 Resolution
Minimum contrast detectable ?

Factory Application site:

Full format: y/n Full format: y/n

Zoom: y/n Zoom: y/n

The minimum contrast must always be visible.

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Checking the control systems 6 6-1

NOTE Perform this test only at the factory.

The following control systems are in operation with the indicated prefiltration:
ADR at approx. 6 mm Cu and dynamic test in the beam path
Iris diaphragm at approx. 8.1 mm Cu and dynamic test in the beam path
AGC at approx. 11.1 mm Cu and dynamic test in the beam path

This test is used to check the operation of these control systems.

Prerequisites
• For SIREMOBIL Compact with 2 monitors, both must be set for approximately the same
(synchronous) brightness and contrast (LUT, brightness and contrast setting).

Preparations
• Test requirements: See chapter1.
• Attach the dynamic test
- without holder,
- with heart contour diaphragm,
- without Plexi capillary test to the image intensifier.
• Select FLUORO: dose rate level "Mid".
• Select Sirematic HC1 ADR curve; the LED of the mA button is off.
• Select LUT1 for both monitors (if existing).
• Select edge enhancement at maximum detectability of bright/dark transitions.
• Switch X-ray image intensifier to full size.
• Open the collimator to maximum aperture.
• Prefilter with copper until 106 kV to 109 kV is displayed.
Switch fluoro on briefly (around 6 mm Cu required).
• Radiation ON.
• Evaluate the brightness of the fluoro image.
• Radiation OFF.

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6-2 Checking the control systems
Evaluation 1
• Attach an additional 2.1mm Cu at the radiation output.
• Radiation ON;
The generator maximum 110kV / 3mA must be attained.
• Store the LIH image as reference image.
• Evaluate the brightness of the fluoro image.
• The brightness with approx. 6mm Cu prefiltration and dynamic test should be
approximately equal to the brightness with 8.1mm Cu and the dynamic test.
Factory
Brightness with ADR and iris diaphragm controll the same? y/n

Evaluation 2
• Attach additional 3mm Cu to the radiation output.
• Radiation ON ;
• Evaluate the brightness of the fluoro image.
• The brightness with approximately 8.1mm Cu prefiltration and dynamic test (stored
reference image) must approximately equal the brightness with approximately 11.1 mm
Cu and dynamic test.
Factory
Brightness with ADR and AVR the same? yn

Programming the previous noted values of the organ programs 6

NOTE Before performing the IQ-Quick-Test, the organ programs were

set in accordance to chapter 1, paragraph Test requirements.
These have to be reprogrammed to the previous noted parameter
values.

Program the organ programs back to the original and previous noted parameter values.

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Image artifacts 7 7-1

Image artifacts 7

• Cross off all image artifacts which have been detected during setting and image quality
tests in the table in the image quality test certificate.
• If any image artifacts are detected which are not listed in the table, these must be
described under ”Other artifacts”.
• To evaluate the respective artifacts, there are three rating numbers which indicate the
extent of each artifact:

Definition of the rating numbers 7

1 = No artifacts could be determined during start-up.

2 = A few artifacts occurred sporadically during start-up. The cause could not be located
and the "error" could not be corrected. The artifacts do not negatively influence the
overall appearance of the images and do not compromise the diagnostic value of the
images in any way. The artifacts are determined to be tolerable.
3 = During start-up, artifacts occurred frequently or with greater severity and they nega-
tively influenced the overall appearance of the images or compromised their diag-
nostic value. Therefore, the artifacts were determined to be intolerable and the
system could not be turned over to the customer.

Description of the artifacts 7

• Hum:
Inhomogeneity caused by electro-magnetic fields in imaging systems. This artifact may
significantly influence the diagnostic value of the images depending on the degree.
Optimally, this artifact should not occur at all, however, extremely low levels can be
tolerated. Hum artifacts appear as periodic, horizontal bright and dark structures in the
image; they appear briefly and are not specific to one location.
• Interference stripes
Very high-frequency electro-magnetic fields appear in the image as bright or dark,
sometimes very short, transverse marks in the image. They appear briefly. Stripes
caused by contaminants on the surfaces of lenses, etc. should be included in this group.
In this case, they are specific to one location and appear constantly. Stripes cannot be
tolerated.
• Ghosting:
These artifacts are object contours displayed twice, with the second contour generally
shifted laterally. They are caused by reflections in long, poorly adjusted video cables.
Clearly visible ghosting cannot be tolerated.
• Background structures are stationary, grid-shaped patterns primarily in dark regions of
the image. They are also referred to as ”standing noise”.
• Pixel errors are image pixels without image information. They are visible on the monitor
as bright and black dots the size of pixels.

Some types of pixel errors can be tolerated while others cannot. The TV camera is
carefully inspected with respect to pixel errors at the TV test bay prior to shipment. TV
cameras can be turned over to the customer only if the number of pixel errors meets the

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7-2 Image artifacts
factory specifications. These pixel errors can be tolerated and must be documented in
the IQ test certificate.

Image artifacts 7

Required value for the assessment of the artifact: Only 1 and 2 can be tolerated

Factory Start-up
Type of artifact Assessment of the artifact*1
1 2 3 1 2 3
Hum
Interference stripes
Ghost images (reflections)
Background structures
Pixel error

*1 Rating number of artifact

1 = No artifacts
2 = Slight artifacts
3 = Disturbances that cannot be tolerated

Remarks:_______________________________________________________________

_______________________________________________________________________

_______________________________________________________________________

_______________________________________________________________________

Other artifacts: 7

_______________________________________________________________________

_______________________________________________________________________

_______________________________________________________________________

_______________________________________________________________________

_______________________________________________________________________

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Customer specific organ programs 8 8-1

Programming the organ programs 8

(Upon customer request only, at the application site.)

The customer has selected the standard organ programs: y/n

If "y": omit this chapter.

SIREMOBIL Compact without keyboard 8

• Connect the service PC to the external service interface.

• Install the Memoskop service program on the service PC using the installation routine on
the diskette.
The service diskettes are located in the Log book, Register 10.
• Call up the Memoskop service program and program the organ programs requested by
the customer.
• Print out the programmed values using the print function in the Memoskop service
program. Sign and date the printout and file it in the customer’s copy of the operating
instructions in the chapter on "Curves and Diagrams."

SIREMOBIL Compact with keyboard 8

The customer can change the organ programs himself using the operating instructions.
The programmed parameters can be read out again by the customer after calling up
"User Setup".

Checking the newly programmed ADR control curves 8

Prerequisites 8

The test of the ADR control curves Sirematic HC1 and Sirematic HC2 was already per-
formed. Refer to chapter 2 of these instructions.
• Select "Mid" as the dose rate level. This corresponds to a dose rate of 0.22 µGy/s ±15%
for a 17 cm (7") I.I. and survey format or 0.185 µGy/s ±15% for a 23 cm I.I. (9") and
survey format.
• If required, program the dose rate levels in the organ programs temporarily to "Mid".

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8-2 Customer specific organ programs
Procedure 8

• Select FLUORO .
• Attach a 2.1 mm Cu prefilter to the radiation output.
• After selecting the respective fluoro organ program and activating the mA key, the
programmed ADR control curves can be selected.
• Switch fluoro ON.

NOTICE Note the programmed dose rate level. To check the newly pro-
grammed ADR control curves, temporarily program the "Mid"
dose rate level (refer above).

Evaluation 8

• Read the kV and mA values displayed on the control panel and enter them for the
associated ADR control curve in table 1.
• Switch fluoro OFF .
• Select any additionally programmed ADR control curves by selecting the corresponding
organ programs and the mA key and enter the kV and mA values in table 1.

ADR- Typical values Actual values on-site

Curve
kV mA kV mA
SIREMATIC LD 80 - 96 02 - 0.4
SIREMATIC S1 67 - 79 0,9 - 1.5
SIREMATIC S2 65 - 75 1.1 - 1.9
SIREMATIC HC1 63 - 68 1.9 - 3.8
SIREMATIC HC2 61 - 66 2.1 - 4.7
IODINE 61 - 65 2.1 - 5.0

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Multispot 2000 9 9-1

Multispot 2000 present? y/n

If "n": chapter not applicable.

Since the Multispot 2000 must be optimally set for the film used and the development
required at the user's site, only a functional test is performed at the factory.

Functional check at the factory 9

The functional check must be performed for all possible image subdivisions, in each case
with positive and negative image display.
Definition: Positive image display means that the hardcopy image is identical with the
monitor display.

Requirements 9

• Select Memory test image (Appendix).

• Set LUT to position 1.
• A camera warm-up period of 20 minutes must be observed.
• Select the image subdivision to be tested in each case.
• Select the image display (positive/negative) to be tested in each case.
• Set the relevant B, C, D values shown in Table 1:

positive image display negative image display

B C D B C D
at 50 Hz at 60 Hz at 50 Hz at 60 Hz
refresh refresh refresh refresh
rate rate rate rate

Multispot 2000 1/4, 008 550 035 042 020 660 035 042
full format
Multispot 2000 1/4, 008 550 016 019 020 660 016 019
4-on-1 image
Multispot 2000-2 008 550 021 025 020 660 021 025

Tab. 1

• Enter the film type used and the emulsion number:

Film type: Kodak EKTASCAN DNB; Emulsion number:________________

• Enter the film density values measured in Table 2.

NOTICE In the case of deviations from the nominal value 2 (film density
40%), B must be corrected (adjusted).

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9-2 Multispot 2000
Mark the fields which are not applicable with n.a.

Setting values Film density

factory function check
B C D Nominal value Factory
MS 2000 1/4 full image, 0% ≤ 0.27
(1)
negative image display 40% 1.0 ± 0.3
(2)
100% ≥ 2.4
(3)
MS 2000 1/4 full image, 0% ≥ 2.4
(1)
positive image display 40% 1.3 ± 0.3
(2)
100% ≤ 0.27
(3)
MS 2000 1/4 4-on-1 image, 0% ≤ 0.27
(1)
negative image display 40% 1.0 ± 0.3
(2)
100% ≥ 2.4
(3)
MS 2000 1/4 4-on-1 image, 0% ≥ 2.4
(1)
positive image display 40% 1.3 ± 0.3
(2)
100% ≤ 0.27
(3)
MS 2000-2, 0% ≤ 0.27
(1)
negative image display 40% 1.0 ± 0.3
(2)
100% ≥ 2.4
(3)
MS 2000-2, 0% ≥ 2.4
(1)
positive image display 40% 1.3 ± 0.3
(2)
100% ≤ 0.27
(3)
Tab. 2

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Multispot 2000 9-3

Setting the multiformat camera at the customer's site 9

The setting must be performed for all possible image subdivisions, in each case with the
image display (positive and/or negative) desired by the customer.
Mark the settings not performed with n.a. in the relevant table.
Definition: Positive image display means that the hardcopy image is identical with the
monitor display.
• Film type used: ______________ Emulsion number: ______________

• Select Memory test image (Appendix).

• A camera warm-up period of 20 minutes must be observed.
• Set LUT to position 1.
• Start the setting procedure with the B, C, D values shown in Table 2.
• Select the image subdivision to be set in each case.
• Select the image display to be set in each case.
• Change B until the 40% gray level (see Fig.1) corresponds to the nominal value for the
film density Dnom. (see Tables 3 to 6).
• Change C until the film density values for white and black correspond to the nominal
values (see Tables 3 to 6).
When increasing the contrast values (C), ensure that the 100% fields and 90% fields and
the 0% fields and 10% fields can be distinguished from one another.

Multispot 2000-2 9

Negative image display

• Enter the values determined in Table 3.
• Enter the values programmed for B, C, and D in Table 3.
Positive image display
• Enter the values determined in Table 4.
• Enter the values programmed for B, C, and D in Table 4.

Multispot 2000 1/4 9

Negative image display

Full-field image (1/1)

• Enter the values determined in Table 3.
• Enter the values programmed for B, C, and D in Table 3.

4-on-1 image (1/4)

• Enter the values determined in Table 5.
• Enter the values programmed for B, C, and D in Table 5.

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9-4 Multispot 2000
Positive image display

Full-field image (1/1)

• Enter the values determined in Table 4.
• Enter the values programmed for B, C, and D in Table 4.

4-on-1 image (1/4)

• Enter the values determined in Table 6.
• Enter the values programmed for B, C, and D in Table 6.

59
/ 1
A B

3 1

Fig. 1

Memory test image on the monitor [Film = Positive image display]

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Multispot 2000 9-5
Application site:
Film density values for Multispot 2000-2 or Multispot 2000 1/4 with full-field image
and negative image display:

Field Film density Film density D Programmed values

nominal values Dnom
0% (1) ≤ 0.25 B
40% (2) 1.0 ± 0.1 C
100% (3) ≥ 2.5 D
Tab. 3

Application site:
Film density values for Multispot 2000-2 or Multispot 2000 1/4 with full-field image
and positive image display:

Field Film density Film density D Programmed values

nominal values Dnom
0% (1) ≥ 2.4 B
40% (2) 1.3 ± 0.1 C
100% (3) ≤ 0.25 D
Tab. 4

Application site:
Film density values for Multispot 2000 1/4 with 4-on-1 and negative image display:

Field Film density Film density D Programmed values

nominal values Dnom
0% (1) ≤ 0.25 B
40% (2) 1.0 ± 0.1 C
100% (3) ≥ 2.5 D
Tab. 5

Application site:
Film density values for Multispot 2000 1/4 with 4-on-1 and positive image display:

Field Film density Film density D Programmed values

nominal values Dnom
0% (1) ≥ 2.4 B
40% (2) 1.3 ± 0.1 C
100% (3) ≤ 0.25 D
Tab. 6

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9-6 Multispot 2000

Checking the Multispot resolution 9

Prerequisites 9

• Select FLUORO (standard settings see Appendix)

- Select Sirematic HC1 ADC control characteristic; the LED of the mA button is off.
• Select image intensifier full format.
• Set contrast setting for monitor B to LUT 1.
• Factory: Resolution test Type 41A; Application site: Resolution test Type 41
• Fasten the resolution test at around 45 degrees inclined to the grid lines in the image
intensifier center directly on the grid.
• Factory: Attach 25 mm AL measuring stand close to the image intensifier.

• Application site: With 25 mm AL measuring stand present (with 0.4 mm notch),

attach this close to the image intensifier.
Otherwise: Fasten 17µm Cu next to the resolution test directly on
the grid and attach 1.2 mm Cu in the beam path close to the tube.

• If overframing occurs at the edge of the image intensifier, mask this out.
• Switch radiation "on" and let it stabilize. Switch radiation "off".
• Transfer (store) the LIH image on monitor B.
• Select negative image display of the Multispot.

Multispot 2000-2 9

• Expose the film (both partial exposures) and develop it.

• Evaluate both partial exposures.
• Enter the lower resolution value in Table 7.
Resolution nominal values [Lp/mm] Resolution actual values [Lp/mm]
negative image display negative image display
7" (17cm) 9" (23cm) Factory Application site
1.4 1.2

Tab. 7

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Multispot 2000 9-7
Multispot 2000-1/4 9

• Expose a film at full format.

• Evaluate the exposure.
• Enter the values determined in Tab. 7.
• Expose a film in 4-on-1 format (all 4 partial exposures).
• Evaluate all 4 partial exposures.
• Enter the lowest resolution value in Tab. 8.

Image format Resolution nominal values [Lp/mm] Resolution actual values [Lp/mm]
negative image display negative image display
7" (17cm) 9" (23cm) Factory Application site
Full format 1.4 1.2

4-on-1 format 1.4 1.2

Tab. 8

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9-8 Multispot 2000
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Final Steps 10 10 - 1
• If the SIREMOBIL Compact covers were removed, perform the protective conductor test
in accordance with ARTD part 2 (CD-ROM).

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10 - 2 Final Steps
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Appendix 11 11 - 1

Calling up the Memoskop test patterns 11

Memoskop CE / CE100 / C / C-SUB / C-SUB & MOD with keyboard 11

You can call up Technical Setup for the memory by pressing CTRL + T.
Various test patterns can be called up from the first menu.

Memoskop CE without keyboard 11

• Connect the service PC to the external service interface.

• Install the Memoskop service program using the installation routine on the diskette.
The service diskettes are located in the log book, Register 10.
• Call up the Memoskop service program in the "Test pattern generation" menu.
Various test patterns can be called up from the menu.

Memoskop CX200 11

You can call up Technical Setup for the memory by pressing CTRL + T.
Various test patterns can be called up from the menu "8 Input Setup".

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11 - 2 Appendix

Standard programming 11

MEMOSKOP CE / CE100 / C / C-SUB / C-SUB & MOD 11

The organ programs are stated with their default values in the operating instructions of the
SIREMOBIL Compact.
The following default values are programmed in organ program 1 when the SIREMOBIL
Compact is delivered:

Organ program1
Operating mode FL IFL DR SUB Roadmap
Program name (*4) Standard Standard Standard Standard Standard
Dose rate MID MID HIGH HIGH HIGH
SIREMATIC normal HC1 HC1 n.a. n.a. n.a.
(DR850W*1) (Iodine) (Iodine)
SIREMATIC push HC2 HC2 n.a. n.a. n.a.
(DR850W*1)
Noise red. Low MD1 K=4 K=8 n.a. n.a.
(K4:K1)
Noise red. High MD2 K=8 K = 16 n.a. n.a.
(K16:K2)
Dose reduction low n.a. high n.a. n.a. n.a.
Dose reduction high n.a. high n.a. n.a. n.a.
Auto LIH disk transfer (*2) NO NO n.a. n.a. n.a.
Auto transfer each image (*2) n.a. NO n.a. n.a. n.a.
Disk transfer rate (*2) 0 n.a. n.a. n.a. n.a.
Auto disk transfer (*2) n.a. NO YES n.a. n.a.
Subtraction (*3) n.a. n.a. n.a. MAX MAX
Landmark (*3) n.a. n.a. n.a. NO NO
Video signal at docum. (*3; *5) n.a. n.a. n.a. POS POS
Image display (*3; *5) n.a. n.a. n.a. POS POS
Duration of the phase B1 (*3) n.a. n.a. n.a. 0 sec n.a.
Disk transfer rate (Phase B1)(*3) n.a. n.a. n.a. 0 n.a.
Disk transfer rate (Phase B2)(*3) n.a. n.a. n.a. 3 n.a.

(*1) Observe a cool-down phase of 30s between 2 sequential DR exposures, otherwise,

the ADR curve DR550W will automatically be selected.
(*2) For Memoskop C with hard disk only.
(*3) For Memoskop C-SUB or Memoskop C-SUB & Mod.

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Appendix 11 - 3

(*4) The name is listed as an example only and can be any program name.
(*5) Image display on film should correspond to image display on the monitor.

SUB & Roadmap

Windows / Level
/1 Brightness 100
/1 Contrast 195
/2 Brightness 105
/2 Contrast 205
/3 Brightness 110
/3 Contrast 215
/4 Brightness 115
/4 Contrast 225
/5 Brightness 120
/5 Contrast 235
/6 Brightness 127
/6 Contrast 245

SUB & Roadmap K-Factors / time

SUB phase A K-Factor 32
SUB phase B K-Factor MD2
SUB phase A time 45
Roadmap phase A K-Factor 32
Roadmap phase B K-Factor MD2
Roadmap phase C K-Factor MD2
Roadmap phase A time 45

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11 - 4 Appendix
MEMOSKOP CX200 11

The organ programs are stated with their default values in the operating instructions of the
SIREMOBIL Compact / L.
The following default values are programmed in organ program 1 when the SIREMOBIL
Compact is delivered:

Organ program 1
Operating mode DL IDL DR SUB Roadmap
Program name Standard Standard Standard SUB 2F/s Standard
Doserate MID MID MID HIGH HIGH
SIREMATIC normal S2 S2 n.a. n.a. n.a.
SIREMATIC push HC2 HC2 n.a. n.a. n.a.
Noise red. Low K=4 K=4 K=8 n.a. n.a.
Noise red. High MD2 K=8 K = 16 n.a. n.a.
Dose reduction low n.a. high n.a. n.a. n.a.
Dose reduction high n.a. mid n.a. n.a. n.a.
Auto LIH disk transfer NO NO n.a. n.a. n.a.
Auto transfer each image n.a. NO n.a. n.a. n.a.
Disk transfer rate 0 n.a. n.a. n.a. n.a.
Auto disk transfer n.a. NO YES n.a. n.a.
Subtraction (*2) n.a. n.a. n.a. MAX MAX
Landmark (*2) n.a. n.a. n.a. NO NO
Video signal at docum. (*2; *3) n.a. n.a. n.a. POS POS
Image display (*2; *3) n.a. n.a. n.a. POS POS
Duration of the phase B1 (*2) n.a. n.a. n.a. 0 sec n.a.
Disk transfer rate phase B1 (*2) n.a. n.a. n.a. 0 n.a.
Disk transfer rate phase B2 (*2) n.a. n.a. n.a. 2 n.a.

(*1) Observe a cool-down phase of 30s between 2 sequential DR exposures, otherwise,

the ADR curve DR550W will automatically be selected.
(*2) For Memoskop CX200 with Option 5000 Images + DSA only.
(*3) Image display on film should correspond to image display on the monitor.

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Appendix 11 - 5

SUB & Roadmap

Windows / Level
/1 Brightness 3120
/1 Contrast 1600
/2 Brightness 3280
/2 Contrast 1680
/3 Brightness 3440
/3 Contrast 1760
/4 Brightness 3600
/4 Contrast 1840
/5 Brightness 3760
/5 Contrast 1920
/6 Brightness 3920
/6 Contrast 2032

SUB & Roadmap K-Factors / time

SUB phase A K-Factor 16
SUB phase B K-Factor 8
SUB phase A time 15
Roadmap phase A K-Factor 16.
Roadmap phase B K-Factor 8
Roadmap phase C K-Factor 8
Roadmap phase A time 15

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Medical Engineering Rev. 04 01.06 CS PS SP Log book
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SIREMOBIL Compact / L Register 5 SPR2-130.037.01 Page 6 of 6 Siemens AG

Log book Rev. 04 01.06 CS PS SP Medical Engineering
Changes to previous version 12 12 - 1

All chapters Revision revised

Chapter 1 Required measuring instruments and devices revised
Test requirements revised.
Chapter 2 bis 6 Test requirements revised.
Chapter 8 Descriptions for Memoskop CX200 added.
Chapter 10 Descriptions for Memoskop CX200 added.
Chapter 11 Descriptions for Memoskop CX200 added.
Chapter 12 Revised

Siemens AG Register 5 SPR2-130.037.01 Page 1 of 2 SIREMOBIL Compact / L

Medical Engineering Rev. 04 01.06 CS PS SP Log book
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SIREMOBIL Compact / L Register 5 SPR2-130.037.01 Page 2 of 2 Siemens AG

Log book Rev. 04 01.06 CS PS SP Medical Engineering